Dissecting the Genetic Complexity of Human 6p Deletion Syndromes by Using a Region-Specific, Phenotype-Driven Mouse Screen

Autor: Bogani, Debora, Willoughby, Catherine, Davies, Jennifer, Kaur, Kulvinder, Mirza, Ghazala, Paudyal, Anju, Haines, Heather, McKeone, Richard, Cadman, Matthew, Pieles, Guido, Schneider, Jürgen E., Bhattacharya, Shoumo, Hardy, Andrea, Nolan, Patrick M., Tripodis, Nikos, Depew, Michael J., Chandrasekara, Ramya, Duncan, Gimara, Sharpe, Paul T., Greenfield, Andy, Denny, Paul, Ragoussis, Jiannis, Arkell, Ruth M., Anderson, Kathryn V.

Publikováno v: Proceedings of the National Academy of Sciences of the United States of America, 2005 Aug . 102(35), 12477-12482.

Externí odkaz: https://www.jstor.org/stable/3376603